Cellular target of weak magnetic fields: ionic conduction along actin filaments of microvilli.

The interaction of weak electromagnetic fields (EMF) with living cells is a most important but still unresolved biophysical problem. For this interaction, thermal and other types of noise appear to cause severe restrictions in the action of weak signals on relevant components of the cell. A recently presented general concept of regulation of ion and substrate pathways through microvilli provides a possible theoretical basis for the comprehension of physiological effects of even extremely low magnetic fields. The actin-based core of microfilaments in microvilli is proposed to represent a cellular interaction site for magnetic fields. Both the central role of F-actin in Ca2+ signaling and its polyelectrolyte nature eliciting specific ion conduction properties render the microvillar actin filament bundle an ideal interaction site for magnetic and electric fields. Ion channels at the tip of microvilli are connected with the cytoplasm by a bundle of microfilaments forming a diffusion barrier system. Because of its polyelectrolyte nature, the microfilament core of microvilli allows Ca2+ entry into the cytoplasm via nonlinear cable-like cation conduction through arrays of condensed ion clouds. The interaction of ion clouds with periodically applied EMFs and field-induced cation pumping through the cascade of potential barriers on the F-actin polyelectrolyte follows well-known physical principles of ion-magnetic field (MF) interaction and signal discrimination as described by the stochastic resonance and Brownian motor hypotheses. The proposed interaction mechanism is in accord with our present knowledge about Ca2+ signaling as the biological main target of MFs and the postulated extreme sensitivity for coherent excitation by very low field energies within specific amplitude and frequency windows. Microvillar F-actin bundles shielded by a lipid membrane appear to function like electronic integration devices for signal-to-noise enhancement; the influence of coherent signals on cation transduction is amplified, whereas that of random noise is reduced.

[1]  Gerald S. Manning,et al.  Limiting Laws and Counterion Condensation in Polyelectrolyte Solutions I. Colligative Properties , 1969 .

[2]  G. S. Manning Limiting laws and counterion condensation in polyelectrolyte solutions. IV. The approach to the limit and the extraordinary stability of the charge fraction. , 1977, Biophysical chemistry.

[3]  R. Fettiplace,et al.  An electrical tuning mechanism in turtle cochlear hair cells , 1981, The Journal of physiology.

[4]  B. Boman,et al.  Cell surface characteristics of proadipocytes growth arrested at the predifferentiation GD state. Defects associated with neoplastic transformation. , 1983, Laboratory investigation; a journal of technical methods and pathology.

[5]  M. Dickens,et al.  Orientation of skeletal muscle actin in strong magnetic fields , 1984, FEBS letters.

[6]  U. Lindberg,et al.  Specific interaction between phosphatidylinositol 4,5-bisphosphate and profilactin , 1985, Nature.

[7]  J. V. May,et al.  Synergistic effect of insulin and follicle-stimulating hormone on biochemical and morphological differentiation of porcine granulosa cells in vitro. , 1988, Biology of reproduction.

[8]  A. J. Hudspeth,et al.  How the ear's works work , 1989, Nature.

[9]  Z. Bielańska-Osuchowska Prenatal development of the adrenal gland in the pig (Sus scrofa domestica). Part I. The differentiation and development of the adrenal cortex primordium in the first half of pregnancy. , 1989, Folia morphologica.

[10]  D. St-Onge,et al.  Evidence of direct interaction between actin and membrane lipids. , 1989, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[11]  I. Zusman,et al.  Effects of pulsing electromagnetic fields on the prenatal and postnatal development in mice and rats: in vivo and in vitro studies. , 1990, Teratology.

[12]  D J Drost,et al.  Time-varying magnetic fields increase cytosolic free Ca2+ in HL-60 cells. , 1990, The American journal of physiology.

[13]  R P Liburdy,et al.  Nonthermal 60 Hz sinusoidal magnetic‐field exposure enhances 45Ca2+ uptake in rat thymocytes: dependence on mitogen activation , 1990, FEBS letters.

[14]  K. Lange,et al.  Restricted localization of the adipocyte/muscle glucose transporter species to a cell surface‐derived vesicle fraction of 3T3‐L1 adipocytes , 1990, FEBS letters.

[15]  T. Pollard,et al.  The actin-binding protein profilin binds to PIP2 and inhibits its hydrolysis by phospholipase C. , 1990, Science.

[16]  R. Astumian,et al.  Activation of Na+ and K+ pumping modes of (Na,K)-ATPase by an oscillating electric field. , 1990, The Journal of biological chemistry.

[17]  F. Papatheofanis Use of calcium channel antagonists as magnetoprotective agents. , 1990, Radiation research.

[18]  W. R. Adey,et al.  Calcium uptake by leukemic and normal T-lymphocytes exposed to low frequency magnetic fields. , 1991, Bioelectromagnetics.

[19]  D. Benos,et al.  Amiloride-sensitive sodium channel is linked to the cytoskeleton in renal epithelial cells. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[20]  T. Pollard,et al.  Regulation of phospholipase C-gamma 1 by profilin and tyrosine phosphorylation. , 1991, Science.

[21]  V. Lednev,et al.  Possible mechanism for the influence of weak magnetic fields on biological systems. , 1991, Bioelectromagnetics.

[22]  J. Ashmore The electrophysiology of hair cells. , 1991, Annual review of physiology.

[23]  T. Budinger,et al.  Pulsed magnetic field effects on calcium signaling in lymphocytes: Dependence on cell status and field intensity , 1992, FEBS letters.

[24]  R. Liburdy,et al.  Time‐varying and static magnetic fields act in combination to alter calcium signal transduction in the lymphocyte , 1992, FEBS letters.

[25]  R. Wondergem,et al.  Mouse hepatocyte membrane potential and chloride activity during osmotic stress. , 1992, The American journal of physiology.

[26]  R P Liburdy,et al.  Calcium signaling in lymphocytes and ELF fields Evidence for an electric field metric and a site of interaction involving the calcium ion channel , 1992, FEBS letters.

[27]  K. Lange,et al.  Rapid uptake of calcium, ATP, and inositol 1,4,5‐trisphosphate via cation and anion channels into surface‐derived vesicles from HIT cells containing the inositol 1,4,5‐trisphosphate‐sensitive calcium store , 1993, FEBS letters.

[28]  C. Sibley,et al.  Transtrophoblast and microvillus membrane potential difference in mature intermediate human placental villi. , 1993, The American journal of physiology.

[29]  M. Engelke,et al.  Fluidity of the microsomal membrane and cytochrome P450 reduction kinetics of pig liver microsomes as a consequence of organic solvent impact. , 1993, Xenobiotica; the fate of foreign compounds in biological systems.

[30]  K. Lange,et al.  The IP3‐sensitive calcium store of HIT cells is located in a surface‐derived vesicle fraction , 1993, FEBS letters.

[31]  R. Liburdy,et al.  Experimental evidence for 60 Hz magnetic fields operating through the signal transduction cascade , 1993, FEBS letters.

[32]  H. Cantiello,et al.  A novel method to study the electrodynamic behavior of actin filaments. Evidence for cable-like properties of actin. , 1993, Biophysical journal.

[33]  Erik Lundgren,et al.  Intracellular calcium oscillations induced in a T‐cell line by a weak 50 Hz magnetic field , 1993, Journal of cellular physiology.

[34]  R. Romand,et al.  Ontogenesis of F-actin in hair cells. , 1993, Cell motility and the cytoskeleton.

[35]  T. Tsong,et al.  Recognition and processing of randomly fluctuating electric signals by Na,K-ATPase. , 1994, Biophysical journal.

[36]  P. Devarajan,et al.  Ankyrin binds to two distinct cytoplasmic domains of Na,K-ATPase alpha subunit. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[37]  B. Neuschwander‐Tetri,et al.  Stable differentiation of a human colon adenocarcinoma cell line by sodium butyrate is associated with multidrug resistance , 1994, Journal of cellular physiology.

[38]  H. Dertinger,et al.  Stochastic resonance as a possible mechanism of amplification of weak electric signals in living cells. , 1994, Bioelectromagnetics.

[39]  Kaplan,et al.  Optical thermal ratchet. , 1995, Physical review letters.

[40]  H. Sackin Review of Mechanosensitive Channels , 1995 .

[41]  H Sackin,et al.  Mechanosensitive channels. , 1995, Annual review of physiology.

[42]  K. H. Mild,et al.  CD45 phosphatase in Jurkat cells is necessary for response to applied ELF magnetic fields , 1995, FEBS letters.

[43]  Derényi,et al.  Cooperative transport of Brownian particles. , 1995, Physical Review Letters.

[44]  K. Hansson Mild,et al.  Low frequency MFs increased inositol 1,4,5‐trisphosphate levels in the Jurkat cell line , 1995, FEBS letters.

[45]  M. McLean,et al.  Measurement and analysis of static magnetic fields that block action potentials in cultured neurons. , 1995, Bioelectromagnetics.

[46]  J. Yager,et al.  A morphological study of differentiated hepatocytes in vitro , 1995, Hepatology.

[47]  A J Hudspeth,et al.  Detection of Ca2+ entry through mechanosensitive channels localizes the site of mechanoelectrical transduction in hair cells. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[48]  B. Veyret,et al.  Stimulation of Ca2+ influx in rat pituitary cells under exposure to a 50 Hz magnetic field. , 1996, Bioelectromagnetics.

[49]  A. Rosen Inhibition of calcium channel activation in GH3 cells by static magnetic fields. , 1996, Biochimica et biophysica acta.

[50]  K. Lange,et al.  Detection of the ATP-dependent nonmitochondrial calcium store in a cell surface-derived vesicle fraction from isolated rat hepatocytes. , 1996, Experimental cell research.

[51]  H. Tähti,et al.  Perturbation of artificial and biological membranes by organic compounds of aliphatic, alicyclic and aromatic structure. , 1996, Toxicology in vitro : an international journal published in association with BIBRA.

[52]  Jay X. Tang,et al.  The Polyelectrolyte Nature of F-actin and the Mechanism of Actin Bundle Formation (*) , 1996, The Journal of Biological Chemistry.

[53]  K. Lange,et al.  Calcium storage and release properties of F‐actin: evidence for the involvement of F‐actin in cellular calcium signaling , 1996, FEBS letters.

[54]  K. Lange,et al.  Activation of calcium signaling in isolated rat hepatocytes is accompanied by shape changes of microvilli. , 1997, Experimental cell research.

[55]  D. Chikvashvili,et al.  Inactivation of a voltage-dependent K+ channel by β subunit: Modulation by a phosphorylation-dependent interaction between the distal C-terminus of a subunit and cytoskeleton , 1997, Neuroscience Letters.

[56]  B. K. Chang,et al.  Enhanced potency of daunorubicin against multidrug resistant subline KB-ChR-8-5-11 by a pulsed magnetic field. , 1997, Anticancer research.

[57]  V. N. Binghy Interference of Ion Quantum States Within a Protein Explains Weak Magnetic Field's Effect on Biosystems , 1997 .

[58]  R. Drucker-Colín,et al.  Extremely low frequency magnetic fields promote neurite varicosity formation and cell excitability in cultured rat chromaffin cells. , 1997, Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology.

[59]  R. Nagel,et al.  Molecular cloning and expression of a chloride channel-associated protein pICln in human young red blood cells: association with actin. , 1997, The Biochemical journal.

[60]  R. Astumian Thermodynamics and kinetics of a Brownian motor. , 1997, Science.

[61]  I. Roninson,et al.  60-Hz electric fields inhibit protein kinase C activity and multidrug resistance gene (MDR1) up-regulation. , 1997, Radiation research.

[62]  K. Lange,et al.  A new concept for risk assessment of the hazards of non-genotoxic chemicals--electronmicroscopic studies of the cell surface. Evidence for the action of lipophilic chemicals on the Ca2+ signaling system. , 1997, The Science of the total environment.

[63]  S. Grimaldi,et al.  Effect of extremely low frequency (ELF) magnetic field exposure on morphological and biophysical properties of human lymphoid cell line (Raji). , 1997, Biochimica et biophysica acta.

[64]  D. Chikvashvili,et al.  Inactivation of a Voltagedependent K+ Channel by β Subunit , 1997, The Journal of Biological Chemistry.

[65]  T. Tsong,et al.  Fluctuation-driven directional flow in biochemical cycle: further study of electric activation of Na,K pumps. , 1997, Biophysical journal.

[66]  M. Fechheimer,et al.  The structure, function, and assembly of actin filament bundles. , 1997, International review of cytology.

[67]  K. Kaibuchi,et al.  Phosphorylation of Moesin by Rho-associated Kinase (Rho-kinase) Plays a Crucial Role in the Formation of Microvilli-like Structures* , 1998, The Journal of Biological Chemistry.

[68]  A. Bretscher,et al.  An Apical PDZ Protein Anchors the Cystic Fibrosis Transmembrane Conductance Regulator to the Cytoskeleton* , 1998, The Journal of Biological Chemistry.

[69]  H P Zenner,et al.  Evidence for Opening of Hair-Cell Transducer Channels after Tip-Link Loss , 1998, The Journal of Neuroscience.

[70]  R. Drucker-Colín,et al.  Neuronal differentiation of chromaffin cells in vitro, induced by extremely low frequency magnetic fields or nerve growth factor: A histological and ultrastructural comparative study , 1998, Journal of neuroscience research.

[71]  P. Janmey,et al.  The polyelectrolyte behavior of actin filaments: a 25Mg NMR study. , 1999, Biochemistry.

[72]  D A Savitz,et al.  Comparative analyses of the studies of magnetic fields and cancer in electric utility workers: studies from France, Canada, and the United States. , 1999, Occupational and environmental medicine.

[73]  K. Lange Microvillar Ca++ signaling: A new view of an old problem , 1999, Journal of cellular physiology.

[74]  A. Saltiel,et al.  Aldolase Mediates the Association of F-actin with the Insulin-responsive Glucose Transporter GLUT4* , 1999, The Journal of Biological Chemistry.

[75]  S. Tsukita,et al.  Direct Involvement of Ezrin/Radixin/Moesin (ERM)-binding Membrane Proteins in the Organization of Microvilli in Collaboration with Activated ERM Proteins , 1999, The Journal of cell biology.

[76]  B. Katzenellenbogen,et al.  Estrogen Receptor Regulation of the Na+/H+ Exchanger Regulatory Factor. , 1999, Endocrinology.

[77]  Baofeng Hu,et al.  Association of the Epithelial Sodium Channel with Apx and α-Spectrin in A6 Renal Epithelial Cells* , 1999, The Journal of Biological Chemistry.

[78]  M. Repacholi,et al.  Interaction of static and extremely low frequency electric and magnetic fields with living systems: health effects and research needs. , 1999, Bioelectromagnetics.

[79]  B. Katzenellenbogen,et al.  Estrogen receptor regulation of the Na+/H+ exchange regulatory factor. , 1999, Endocrinology.

[80]  R. Liburdy Calcium signaling in lymphocytes and ELF fields: evidence for an electric field metric and a site of interaction involving the calcium ion channel. , 2000, FEBS letters.

[81]  K. Lange Microvillar ion channels: cytoskeletal modulation of ion fluxes. , 2000, Journal of theoretical biology.

[82]  K. Lange Regulation of cell volume via microvillar ion channels , 2000, Journal of cellular physiology.

[83]  Three dimensional (3D) analysis of the morphological changes induced by 50 Hz magnetic field exposure on human lymphoblastoid cells (Raji). , 2000, Bioelectromagnetics.

[84]  K. Lange,et al.  Microvillar cell surface as a natural defense system against xenobiotics: a new interpretation of multidrug resistance. , 2001, American journal of physiology. Cell physiology.

[85]  R. Fettiplace,et al.  Clues to the cochlear amplifier from the turtle ear , 2001, Trends in Neurosciences.

[86]  Y. Hirasawa,et al.  Drug resistance modification using pulsing electromagnetic field stimulation for multidrug resistant mouse osteosarcoma cell line. , 2001, Anticancer research.

[87]  A J Hudspeth,et al.  Compressive nonlinearity in the hair bundle's active response to mechanical stimulation , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[88]  C. Aldinucci,et al.  Pulsed electromagnetic fields affect the intracellular calcium concentrations in human astrocytoma cells , 2001, Bioelectromagnetics.

[89]  Geoffrey A. Manley,et al.  In vivo evidence for a cochlear amplifier in the hair-cell bundle of lizards , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[90]  S. Grimaldi,et al.  Effects of extremely low frequency (50 Hz) magnetic field on morphological and biochemical properties of human keratinocytes , 2002, Bioelectromagnetics.

[91]  P. Villeneuve,et al.  Brain cancer and occupational exposure to magnetic fields among men: results from a Canadian population-based case-control study. , 2002, International journal of epidemiology.

[92]  L. Mirossay,et al.  Effects of static magnetic field on human leukemic cell line HL-60. , 2002, Bioelectrochemistry.

[93]  Kening Wang,et al.  Hepatocyte water volume and potassium activity during hypotonic stress , 1993, The Journal of Membrane Biology.

[94]  M. Gastineau,et al.  Antigenic expression of aminopeptidase M, dipeptidyl-peptidase IV and endopeptidase by primary cultures from rabbit kidney proximal tubule , 2004, Histochemistry.

[95]  U. Thurm,et al.  Cupula displacement, hair bundle deflection, and physiological responses in the transparent semicircular canal of young eel , 1989, Pflügers Archiv.

[96]  F. P. Magee,et al.  Combined magnetic fields increased net calcium flux in bone cells , 1994, Calcified Tissue International.

[97]  A. Mariñoa,et al.  Resting potential of excitable neuroblastoma cells in weak magnetic fields , 2022 .